Annals of Medicine and Surgery 17 (2017) 54e60
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Minimally invasive esophagectomy for esophageal cancer according to the location of the tumor: Experience of 251 patients Lei Chen a, 1, Xi Liu a, 1, Rong Wang b, Yuncang Wang c, Tao Zhang a, Dewei Gao b, *, Linggen Gao b, ** a b c
Department of Thoracic Surgery, General Hospital of Chinese People's Liberation Army, Beijing 100853, China Department of Comprehensive Surgery, General Hospital of Chinese People's Liberation Army, Beijing 100853, China Department of Thoracic Surgery, West China Hospital Chengban Branch Chengdu, Sichuan, 610041, China
h i g h l i g h t s Mid and lower esophageal cancers occurred in most of included patients. MIE Ivor Lewis approach is used for the treatment of mid and lower esophageal cancers. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. MIE according to the location of the tumor decrease postoperative complications.
a r t i c l e i n f o
a b s t r a c t
Article history: Received 25 January 2017 Received in revised form 30 March 2017 Accepted 30 March 2017
Background: Minimally invasive esophagectomy (MIE) is increasingly used for the treatment of esophageal cancer. However, the ideal approach of MIE is not yet standardized. We explore the ideal approach of MIE according to the location of the tumor and compare the clinical outcomes between patients with cancer arising in the upper third of the esophagus and those with tumors involving the middle and lower third of the esophagus. Methods: We included patients with esophageal carcinoma and had clear indications for MIE. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted. Results: Of the 251 patients included in this analysis, 200 patients underwent Ivor-Lewis MIE and 51 patients underwent McKeown MIE. The incidence of anastomotic leak, anastomotic stenosis and recurrent laryngeal nerve injury was significantly higher in the McKeown MIE group than that in the Ivor Lewis MIE group. The 30-day postoperative mortality rate was 1.2% (n ¼ 1) in the McKeown MIE group. Lymph nodes harvested were significantly more in the MIE-McKeown group than in Ivor Lewis MIE group (P < 0.05). The median follow-up period was 15 months (1e25 months) and the overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage 1), 83.8% (stage II), 73.4% (stage III). Conclusions: MIE for esophageal cancer according to the location and clinical stage of the tumor will decrease all postoperative complications and may yield the greatest benefit from surgery. © 2017 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Esophageal cancer Esophagectomy laparoscopy Thoracoscopy
1. Introduction Cancers arising from the esophagus are relatively common in
* Corresponding author. ** Corresponding author. E-mail addresses: [email protected] (D. Gao), [email protected] (L. Gao). 1 Drs. Chen and Liu contributed equally to this work.
China. Surgery is the primary therapy for esophageal cancer. However, traditional open esophagectomy carries significantly high risks of operative morbidity and mortality. Advances in surgical treatment have made minimally invasive esophagectomy (MIE) more popular and widely acceptable since the 1990s [1,2]. Currently, MIE can be performed through the laparoscopic transhiatal, the laparoscopicthoracoscopic Ivor Lewis, or the laparoscopic-thoracoscopic McKeown approach [3]. The prognosis for esophageal cancer is very poor with the
http://dx.doi.org/10.1016/j.amsu.2017.03.038 2049-0801/© 2017 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
median survival time ranging from 1 to 2 years [4]. Traditional open surgical transthoracic and transhiatal esophagectomies are associated with a relatively high morbidity and mortality rate which can impair quality of life [5,6]. In an effort to improve the outcomes associated with esophagectomy, minimally invasive approach to esophageal resection has been adopted [7e11]. The use of MIE approaches was associated with a shorter hospital stay, decreased morbidity and improved outcomes compared with open esophagectomy [12e18]. However, the rapid worldwide use of MIE approaches has not been followed by a rigorous scientific analysis of results. Large scale multicenter surgical clinical trials are difficult to conduct, and few studies have had sufficient follow-up to judge the long-term oncologic results. The numerous technical variables (including the patient's position - prone vs supine or the transoral anvil introduction vs the transthoracic route during an Ivor-Lewis esophagectomy) have jeopardized the results [19]. The ideal approach of MIE is not yet standardized. The potential benefits of McKeown MIE are a more proximal resection margin and improved lymph node dissection. However, these procedures are associated with a high complication rate and mortality, which is partly due to subtotal resection of esophagus, severe trauma, RLN injury and anastomotic leak, and stricture. And one recent study found that McKeown esophagectomy was an independent predictor of increased perioperative morbidity or mortality, independent of tumor histology. There are some advantages for MIE Ivor-Lewis approach such as the avoidance of subtotal resection of esophagus, the lower anastomotic leakage and stenosis, the better vascular supply of gastric conduit, and preliminarily good clinical outcomes. With the development of operative technic, the MIE Ivor-Lewis has become increasingly prevalent and is safe and feasible for patients with mid and lower esophageal cancer. In the present era of minimally invasive surgery, the choice among these approaches is mainly dominated by institutional preferences and clinical opinions. Until recently, the ideal approach of MIE is not yet standardized. The optimal approach should be tailored for each patient according to the location and clinical stage of the tumor [20]. The purpose of this study was to evaluate the effects of MIE approach according to the location of the tumor and to compare differences in perioperative and long term clinical outcomes between patients with cancer arising in the upper third of the esophagus and those with tumors involving the middle and lower third of the esophagus. 2. Patients and methods 2.1. Study design This was a prospective observation trial to evaluate the feasibility and outcomes of tailored therapy for each patient according to the location and the clinical stage of the tumor in an institution that had experience in minimally invasive surgical techniques. Feasibility was defined as the ability to carry out therapy without significant perioperative mortality. Patients included were those scheduled for MIE surgery at the Department of thoracic surgery Chinese PLA General Hospital. from January 2014 onwards. The medical charts were reviewed to obtain clinical data by using a standardized data collection sheet. Variables recorded included sex, age at the time of surgery, comorbid conditions, preoperative symptoms, operative details, and tumor-specific variables. All patients underwent esophagus-gastro-duodenoscopy, a thoracoabdominal CT scan and selective endoscopic ultrasound evaluation every 6 months. All the data was stored in a database that was analyzed for perioperative complications and long term outcomes in patients. The study was approved by the Ethics Committee of Chinese PLA General Hospital, Beijing, China.
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2.2. Pretreatment staging All patients underwent pretreatment staging according to the American Joint Committee on Cancer seventh edition criteria. Diagnostic investigations routinely included a history taking, physical examination, routine laboratory tests, a barium study and an oesophago-gastro-duodenoscopy with biopsies, a neck and thoracoabdominal CT scan, selective endoscopic ultrasound evaluation, and external ultrasonography of the neck, with fine-needle aspiration of lymph nodes when cancer was suspected. 2.3. Eligibility criteria Patients who were histologically proved suffering from esophageal carcinoma by taking biopsy specimens from the tumor during an endoscopy and the stomach was required to be available for use as a conduit were eligible for inclusion in the study. Patients with tumors of no clinical evidence of metastatic spread (M0) were enrolled. A complete evaluation of cardiac and respiratory functions was made, and all patients were found fit for operation and anesthesia. Informed consent was obtained from all patients. Exclusion criteria included patients with a prior antireflux or gastric operation. Patients who had a prior right thoracotomy or a prior major neck operation were excluded. Patients who were converted to an open procedure were also excluded. 2.4. Operative approach For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted (Group A). For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed (Group B). The distance between the incisal edge and the upper edge of the tumor is 5e7 cm. The operative technique has previously been described in detail elsewhere [21e24]. Two main operative techniques are adopted at our institution, namely a three-incision MIE with cervical anastomosis (MIE McKeown approach) and a two-incision MIE with intrathoracic anastomosis (MIE Ivor Lewis approach). After general anesthesia and endotracheal intubation, the patient was placed in the left lateral decubitus position. The surgeon stands on the right and the assistant on the left. Three ports were placed in the 7th intercostal space at mid-axillary line, the 5th intercostal space at the anterior axillary line and in scapular line at the 8th intercostal space respectively. In short, MIE McKeown approach consists of mobilizing the thoracic esophagus from the hiatus to the thoracic inlet, intrathoracic lymphadenectomy and cervical anastomosis. A staging laparoscopy was performed in the same setting or as a separate procedure to ensure resectability in most patients. Neck wound is closed in layers after placing a corrugated drain. Laparoscopic and thoracoscopic dissection is also performed and followed by a side-to-side stapled thoracic anastomosis for the MIE Ivor Lewis approach [12]. Lymph nodes along left gastric artery and the lesser curvature of the stomach, mediastinal lymph nodes, abdominal lymph nodes that included paracardial lymph nodes, with bilateral recurrent nerve lymph nodes were routinely dissected. If the primary tumor was located between the upper and mid-thoracic esophagus, supraclavicular lymph nodes were dissected simultaneously. A feeding jejunostomy tube is placed laparoscopically in most of the patients. One tube-drain is placed close to hiatus, trocars are removed, and ports are closed. Patients are extubated in the operating room. The patients post-operation were given parenteral nutrition through the deep vein or through a nasogastric tube. Patients are discharged on tube feed support with a full liquid diet.
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For patients with positive lymph node metastasis in a resected specimen, adjuvant chemotherapy using 5-fluororouracil and cisplatin every 3 weeks for two cycles was administered.
Survival curves during follow-up were plotted by the Kaplane Meier method. Significance was considered to be present for values of p < 0.05. A commercial statistical software package (SPSS for Windows, version 17.0; SPSS, Chicago, IL) was used for data analysis.
2.6. Perioperative and postoperative outcomes
3. Results
All patients surviving operation were followed until death or time of database closure (January 2016). Perioperative and postoperative data were record, including duration of surgery, blood loss, and postoperative length of stay, surgical outcomes, postoperative complications, operative mortality, recurrence and hospital and late morbidity and mortality. The primary endpoint of this study was all cause mortality. Secondary endpoints were operative and postoperative major morbidity.
3.1. Participants
2.5. Adjuvant chemotherapy
2.7. Statistical analysis Data are reported as the mean ± SD for continuous variables and as frequencies for categorical variables. Continuous variables were compared by Student t-test for normally distributed values. Differences in percentages were evaluated using the Chi-square test.
The study was started in January 2014. We enrolled 258 patients. Two patients were converted to open surgery for bleeding. One patient withdrew consent after registration. Of the remaining 255 patients, two patients had a prior right thoracotomy, one patient had a prior gastric operation, and one patient did not undergo resection, leaving 251 patients eligible for the analysis (Fig. 1). Clinical characteristics of the patients with tumor arising in the middle and lower third of the esophagus (Group A) and the patients with esophageal cancer arising in the upper third of the esophagus (Group B) are listed in Table 1. The total number of included cases was 251, and the male/female ratio was approximately 4:1. At presentation, 47 patients had comorbid conditions in the form of diabetes and 49 patients suffered from coronary artery disease. Of
Fig. 1. Consort diagram.
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
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Table 1 Characteristics of patients who underwent esophagectomy: Comparing MIE-McKeown and MIE-Ivor Lewis. Preoperative characteristics
Group A (n ¼ 200)
Group B (n ¼ 51)
Total, n ¼ 251
P
Age (years) Sex (Male) BMI, kg/m2, median (IQR) Pretreatment weight loss, n (%) Comorbid conditions History of gastroesophageal reflux disease Diabetes mellitus, n (%) Coronary artery disease, n (%) COPD/emphysema, n (%) Chronic renal insufficiency, baseline Cr > 2 mg/dL or HD, n (%) Smoking history Current Former Never
59.9 ± 8.4 169 (84.5%) 23.5 (20.1e26.8) 81 (40.5)
61.4 ± 9.1 38 (74.7%) 22.9 (20.8e25.4) 20 (38.6)
60.4 ± 8.7 207 (82.5%) 23.1 (21.0e26.8) 101 (40.2)
0.192 0.102 0.134 1.000
152 (76.0) 37 (18.5) 40 (20.0) 44 (22.0) 4 (2.0)
40 (78.4) 10 (19.6) 9 (17.6) 12 (23.5) 1 (2.0)
192 (76.9) 47 (18.7) 49 (19.5) 56 (22.3) 5 (2.0)
0.854 0.842 0.844 0.851 1.000
28 (14) 118 (59.0) 54 (27.0)
6 (11.7) 24 (47.1) 21 (41.2)
34 (13.6) 142 (56.6) 75 (29.8)
0.820 0.202 0.059
BMI indicates body mass index; HD, hemodialysis.
the 251 patients with esophageal cancer, 155 (61.7%) patients had dysphagia. All patients were histologically proved suffering from esophageal carcinoma and had clear indications and clinical purpose for MIE. Preoperative nutrition of these patients was maintained by high protein calorie liquid or soft diet. The demographic characteristics were similar between two groups.
chylothorax, cardiac arrhythmia, ICU length of stay and hospital length of stay between two groups. There were no intraoperative mortalities. The 30-day postoperative mortality rate was 1.2% (n ¼ 1) in the McKeown MIE group. This patient died of multiple organ dysfunction syndromes resulting from anastomotic leakage which was confirmed by gastrograf in swallow.
3.2. Operative and postoperative details 3.3. Pathologic findings For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted. Intraoperative and postoperative data of patients are presented in Table 2. Anastomotic leak was detected in eight patients. The leak was minor and managed conservatively. Three patients experienced hoarseness of voice reflecting recurrent laryngeal injury (paresis), which resolved within 5 weeks. Three patients (1.2%) required conversion to open thoracotomy due to adhesions or emergency thoracotomy for bleeding. One patient died of anastomotic leakage postoperatively. Twelve patients experienced long-term complications in the form of stenosis, with dysphagia that required serial dilations. The mean operative time of McKeown MIE group is significant shorter than the Ivor Lewis MIE group (296.1 ± 35.9s vs. 322.8 ± 50.5s, p ¼ 0.013, respectively). However, the occurrence of anastomotic leak, anastomotic stenosis and RLN injury in the McKeown MIE group was significant higher than those in the Ivor Lewis MIE group. There was no statistical significance with the blood loss, adequacy of cancer resection, reoperations, disparity of
Table 2 Technical and perioperative aspects of patients: Comparing MIE-Ivor Lewis and MIEMcKeown.
Duration of surgery (min) Blood loss (ml) Conversion to open, n (%) Reoperations, n (%) Anastomotic leakage, n (%) Anastomotic stenosis, n (%) RLN injury, n (%) Pulmonary complications Chylothorax, n (%) Cardiac arrhythmia, n (%) ICU stay, n (%) Hospital length of stay (d) Mortality at 30 days, n (%) RLN, recurrent laryngeal nerve.
Group A (n ¼ 200)
Group B (n ¼ 51)
P
322.8 ± 50.5 181.5 ± 80.0 2 (1.0) 2 (1.0) 1 (0.5) 2 (1.0) 0 (0) 10 (5.0) 0 (0) 6 (3.0) 3 (1.5) 16.7 ± 5.5 0 (0)
296.1 ± 35.9 172.6 ± 90.1 1 (2.0) 2 (3.9) 4 (7.8) 6 (11.8) 3 (5.9) 8 (15.7) 1 (1.9) 2 (3.9) 2 (3.9) 18.6 ± 6.5 1 (2.0)
0.013 0.594 0.496 0.184 0.007 0.001 0.008 0.103 0.203 0.666 0.268 0.621 0.203
For 215 patients (85.7%), the malignancy was squamous cell cancer. Twenty-eight patients (11.2%) had adenocarcinoma. Six patients had neuroendocrine carcinoma. The remaining 2 patients had Melanoma (Table 3). Lymph nodes harvested were significantly more in the MIE-McKeown group than that of in Ivor Lewis MIE group (P < 0.05). There was no significant difference in the R0 resection rate between groups A and B (95.0%vs. 96.1%). As shown in Table 3, 129 patients were pathologically positive for LN metastasis, which was evaluated as an indication for adjuvant chemotherapy. Of these 129 patients, 98 (76%) received adjuvant chemotherapy. The remaining 31 (24%) patients did not receive chemotherapy because of age (n ¼ 12, 9.3%), other cancer diagnosis (n ¼ 8, 6.2%), postoperative complications (n ¼ 6, 4.7%), and patient's instances (n ¼ 5, 3.9%). 3.4. Clinical outcomes Follow-up was 100% complete in 251 patients. No patient was lost to follow-up. The median follow-up period was 15 months (range, 1e25 months). The overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage I), 83.8% (stage II), 73.4% (stage III). Survival by pathological stage is demonstrated in Fig. 2. Survival by pathological stage and operation procedures are demonstrated in Figs. 3 and 4. Recurrence was mainly systemic in the form of liver and lung metastasis. At this writing, no patient has had any intrathoracic recurrence. 4. Discussion This experience has demonstrated that MIE can be performed safely without intraoperative mortality, with ICU stay rate of 2.0% (n ¼ 5) and a median hospital stay of 17 days. MIE procedure was better than most published series of open esophagectomy [5]. In our comparison of short-term and long-term outcomes between the MIE-chest and MIE-neck groups, the mean operative time of McKeown MIE group is significant shorter than the Ivor Lewis MIE group (p ¼ 0.013). However, the occurrence of anastomotic leak,
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L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60 Table 3 Pathologic findings after operation: Comparing MIE-Ivor Lewis and MIE-McKeown. Tumor specific variables AJCC stage, n (%) I IIa IIb III Squamous tumor type, n (%) Adenocarcinoma tumor type, n (%) Neuroendocrine carcinoma, n (%) Melanoma, n (%) Adequacy of cancer resection Negative margins, n (%) Lymph nodes harvested(n) Lymph nodes metastasis rate, n (%) Adjuvant chemotherapy n (%)
Group A (n ¼ 200)
Group B (n ¼ 51)
P
20 (10.0) 53 (26.5) 48 (24.0) 99 (49.5) 170 (85.0) 24 (12.0) 4 (2.0) 2 (1.0)
7 (13.7) 11 (21.6) 11 (21.6) 22 (43.1) 45 (88.2) 4 (7.9) 2 (3.9) 0 (0)
0.451 0.590 0.854 0.437 0.659 0.618 0.605 1.000
190 (95.0) 19.5 ± 9.6 105 (52.5) 80 (40.0)
49 (96.1) 27.5 ± 10.1 24 (47.1) 18 (35.3)
0.496 0.031 0.532 0.562
AJCC, American Joint Committee on Cancer.
Fig. 2. KaplaneMeier plot of the estimated overall survival of patients stratified by stage.
anastomotic stenosis and RLN injury in the McKeown MIE group was significant higher than those in the Ivor Lewis MIE group. These findings are consistent with the first prospective multicenter study of MIE [7]. In the present study, we choose the approach of MIE according to the location of the tumor. Ivor-Lewis MIE approach is used for the treatment of mid and lower esophageal cancers, and with fewer complications such as RLN injury, anastomosis leak and anastomosis stenosis. These findings are consistent with other reported studies [12,24e28]. The lower rate of anastomosis leak in the MIE Ivor-Lewis group mainly due to the reduced tension at the anastomosis and the ability to remove the potentially ischemic gastric tip. However, Ivor-Lewis MIE is technically demanding and requires extensive experience. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed in our study. The main cause is the intrathoracic anastomosis and the embedding of the staple line in the MIE Ivor-Lewis group are more complex and waste more time. Significantly, more lymph nodes were resected in patients who underwent McKeown MIE in the present study (P < 0.05). The extent of lymph node dissection required for patients with esophageal cancer also remains controversial [29,30]. However,
Fig. 3. KaplaneMeier plot of the estimated overall survival of patients who accepted MIE-Ivor Lewis operation, stratified by stage.
Fig. 4. KaplaneMeier plot of the estimated overall survival of patients who accepted MIE-McKeown operation, stratified by stage.
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
adequate lymph node sampling is required for accurate staging [30]. One of the potential advantages of the McKeown MIE approach is better exposure and improved cervical lymphadenectomy. Esophagectomy is a complex and technically challenging operation. Specialty training of the surgeon and surgeon volume has an impact on clinical outcomes. In the current study, the operative time was significantly different between two groups (322.8 ± 50.5vs. 296.1 ± 35.9) because the intrathoracic anastomosis and the embedding of the staple line in the MIE Ivor-Lewis group were more complex and wasted more time. Intrathoracic anastomosis is technically demanding and learning curve is relatively long. McKeown approach avoids the most difficult problem of intrathoracic anastomosis. Cervical anastomosis is relatively simple and easy to operate. Thus, the MIE McKeown approach is more convenient and easier to grasp for the beginners. In the reports of experienced centers, open esophagectomy approaches are frequently associated with significant morbidity and a mortality rate in the range of 6e23% [31,32]. In one study of 1777 patients undergoing open esophagectomy, the most frequent reported complications were pneumonia (21%), respiratory failure (16%) and prolonged ventilator support (22%) [33]. Given concerns over this high morbidity and mortality, minimally invasive esophagectomy has been performed with increasing frequency. Our mortality of 0.4% and the low incidence of pneumonia (7.17%) and RLN injury (1.2%) suggest an advantage for the MIE. At a median follow-up of 15 months, no significant difference in survival was noted between the two groups of patients. The overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage I), 83.8% (stage II), 73.4% (stage III). Furthermore, the oncological outcomes in the current study were good with an estimated 1-year overall survival of 81.7%. The estimated overall survival is acceptable when compared with published series of open esophagectomy. These results suggest that MIE can provide equivalent oncological outcomes as compared with open transthoracic esophagectomy.
4.1. Strength and limitations The study is prospective trial designed to investigate the effects of MIE approach according to the location of tumor and compare the clinical outcomes between the Ivor Lewis and McKeown MIE procedures. However, there are several limitations in this study. Firstly, the main problem is the relative low proportion of upper third of the esophagus, thus may limited the statistical power. Secondly, the optimal approach to esophagectomy is controversial. The selection of MIE approach is lack of standard and is mainly based on the location of the tumor. Thirdly, the median follow-up period was short and lack of exploration of the long-term effects, especially on quality of life. Longer follow-up period is required to fully evaluate the oncologic results of MIE. it is a single-institution study. Largescale, prospective multicenter trials are required to fully judge the long-term results of MIE.
Ethical approval The study was approved by the Ethics Committee of Chinese PLA General Hospital, Beijing, China.
Sources of funding This work was supported by a general financial grant from the China Postdoctoral Science Foundation (2012T50865, to L. Gao.).
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Author contribution Chen L, Gao LG, Wang R, Liu X and Gao DW contributed to the study design, data collections. Chen L, Zhang T, Liu X contributed to the data analysis, writing. Conflicts of interest The authors declare no conflict of interest. Guarantor Gao DW. Research registration unique identifying number (UIN) Researchregistry1949. Acknowledgment This work was supported by a general financial grant from the China Postdoctoral Science Foundation (2012T50865, to L. Gao.). References [1] O.J. McAnena, J. Rogers, N.S. Williams, Right thoracoscopically assisted oesophagectomy for cancer, Br. J. Surg. 81 (1994) 236e238. [2] S. Law, M. Fok, K.M. Chu, J. Wong, Thoracoscopic esophagectomy for esophageal cancer, Surgery 122 (1997) 8e14. [3] B.A. Yerokun, Z. Sun, C.F. Jeffrey Yang, B.C. Gulack, P.J. Speicher, M.A. Adam, et al., Minimally invasive versus open esophagectomy for esophageal cancer: a population-based analysis, Ann. Thorac. Surg. 102 (2016) 416e423. [4] A. Ayiomamitis, Epidemiology of cancer of the esophagus in Canada: 19311984, Gastroenterology 94 (1988) 374e380. [5] S.H. Bailey, D.A. Bull, D.H. Harpole, J.J. Rentz, L.A. Neumayer, T.N. Pappas, et al., Outcomes after esophagectomy: a ten-year prospective cohort, Ann. Thorac. Surg. 75 (2003) 217e222 discussion 22. [6] J.D. Birkmeyer, A.E. Siewers, E.V. Finlayson, T.A. Stukel, F.L. Lucas, I. Batista, et al., Hospital volume and surgical mortality in the United States, N. Engl. J. Med. 346 (2002) 1128e1137. [7] J.D. Luketich, A. Pennathur, Y. Franchetti, P.J. Catalano, S. Swanson, D.J. Sugarbaker, et al., Minimally invasive esophagectomy: results of a prospective phase II multicenter trial-the eastern cooperative oncology group (E2202) study, Ann. Surg. 261 (2015) 702e707. [8] J.D. Luketich, M. Alvelo-Rivera, P.O. Buenaventura, N.A. Christie, J.S. McCaughan, V.R. Litle, et al., Minimally invasive esophagectomy: outcomes in 222 patients, Ann. Surg. 238 (2003) 486e494 discussion 94e95. [9] T. Irino, J.A. Tsai, J. Ericson, M. Nilsson, L. Lundell, I. Rouvelas, Thoracoscopic side-to-side esophagogastrostomy by use of linear stapler-a simplified technique facilitating a minimally invasive Ivor-Lewis operation, Langenbecks Arch. Surg. 401 (2016) 315e322. [10] S. Sihag, A.S. Kosinski, H.A. Gaissert, C.D. Wright, P.H. Schipper, Minimally invasive versus open esophagectomy for esophageal cancer: a comparison of early surgical outcomes from the society of thoracic surgeons national database, Ann. Thorac. Surg. 101 (2016) 1281e1289. [11] P. Xiao, X. Zhuang, Y. Shen, Q. Li, W. Dai, X.J. Yang, et al., Reverse-puncture anastomotic technique for minimally invasive Ivor-Lewis esophagectomy, Ann. Thorac. Surg. 100 (2015) 2372e2375. [12] J.D. Luketich, A. Pennathur, O. Awais, R.M. Levy, S. Keeley, M. Shende, et al., Outcomes after minimally invasive esophagectomy: review of over 1000 patients, Ann. Surg. 256 (2012) 95e103. [13] M.R. Xie, C.Q. Liu, M.F. Guo, X.Y. Mei, X.H. Sun, M.Q. Xu, Short-term outcomes of minimally invasive Ivor-Lewis esophagectomy for esophageal cancer, Ann. Thorac. Surg. 97 (2014) 1721e1727. [14] K. Kim, J.S. Park, H. Seo, Early outcomes of video-assisted thoracic surgery (VATS) Ivor Lewis operation for esophageal squamous cell carcinoma: the extracorporeal anastomosis technique, Surg. Laparosc. Endosc. Percutan Tech. 23 (2013) 303e308. [15] J. Mu, Z. Yuan, B. Zhang, N. Li, F. Lyu, Y. Mao, et al., Comparative study of minimally invasive versus open esophagectomy for esophageal cancer in a single cancer center, Chin. Med. J. Engl. 127 (2014) 747e752. [16] C. Palanivelu, A. Prakash, R. Senthilkumar, P. Senthilnathan, R. Parthasarathi, P.S. Rajan, et al., Minimally invasive esophagectomy: thoracoscopic mobilization of the esophagus and mediastinal lymphadenectomy in prone positioneexperience of 130 patients, J. Am. Coll. Surg. 203 (2006) 7e16. [17] A.I. Lazzarino, K. Nagpal, A. Bottle, O. Faiz, K. Moorthy, P. Aylin, Open versus minimally invasive esophagectomy: trends of utilization and associated
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thoracoscopic Ivor Lewis esophagectomy for esophageal cancer: initial experience from China, Chin. Med. J. Engl. 125 (2012) 1376e1380. R. Zhang, N. Kang, W. Xia, Y. Che, J. Wan, Z. Yu, Thoracoscopic purse string technique for minimally invasive Ivor Lewis esophagectomy, J. Thorac. Dis. 6 (2014) 148e151. G. Shen, S.B. Pan, M. Wu, S. Zhang, X.F. Xu, G. Chen, Use of efficient pursestring stapling technique for esophagogastric anastomosis in minimally invasive Ivor Lewis esophagectomy, J. Thorac. Dis. 5 (2013) 898e901. T. Lerut, P. Nafteux, J. Moons, W. Coosemans, G. Decker, P. De Leyn, et al., Three-field lymphadenectomy for carcinoma of the esophagus and gastroesophageal junction in 174 R0 resections: impact on staging, disease-free survival, and outcome: a plea for adaptation of TNM classification in upperhalf esophageal carcinoma, Ann. Surg. 240 (2004) 962e972 discussion 72e4. N. Rizk, E. Venkatraman, B. Park, R. Flores, M.S. Bains, V. Rusch, et al., The prognostic importance of the number of involved lymph nodes in esophageal cancer: implications for revisions of the American Joint Committee on Cancer staging system, J. Thorac. Cardiovasc Surg. 132 (2006) 1374e1381. D.P. Kelsen, R. Ginsberg, T.F. Pajak, D.G. Sheahan, L. Gunderson, J. Mortimer, et al., Chemotherapy followed by surgery compared with surgery alone for localized esophageal cancer, N. Engl. J. Med. 339 (1998) 1979e1984. J.D. Birkmeyer, A.E. Siewers, E.V.A. Finlayson, T.A. Stukel, F.L. Lucas, Batista, et al., Hospital volume and surgical mortality in the United States, N. Engl. J. Med. 346 (2002) 1128e1137. S.H. Bailey, D.A. Bull, D.H. Harpole, J.J. Rentz, L.A. Neumayer, T.N. Pappas, et al., Outcomes after esophagectomy: a ten-year prospective cohort, Ann. Thorac. Surg. 75 (2003) 217e222.
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Minimally invasive esophagectomy for esophageal cancer according to the location of the tumor: Experience of 251 patients Lei Chen a, 1, Xi Liu a, 1, Rong Wang b, Yuncang Wang c, Tao Zhang a, Dewei Gao b, *, Linggen Gao b, ** a b c
Department of Thoracic Surgery, General Hospital of Chinese People's Liberation Army, Beijing 100853, China Department of Comprehensive Surgery, General Hospital of Chinese People's Liberation Army, Beijing 100853, China Department of Thoracic Surgery, West China Hospital Chengban Branch Chengdu, Sichuan, 610041, China
h i g h l i g h t s Mid and lower esophageal cancers occurred in most of included patients. MIE Ivor Lewis approach is used for the treatment of mid and lower esophageal cancers. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. MIE according to the location of the tumor decrease postoperative complications.
a r t i c l e i n f o
a b s t r a c t
Article history: Received 25 January 2017 Received in revised form 30 March 2017 Accepted 30 March 2017
Background: Minimally invasive esophagectomy (MIE) is increasingly used for the treatment of esophageal cancer. However, the ideal approach of MIE is not yet standardized. We explore the ideal approach of MIE according to the location of the tumor and compare the clinical outcomes between patients with cancer arising in the upper third of the esophagus and those with tumors involving the middle and lower third of the esophagus. Methods: We included patients with esophageal carcinoma and had clear indications for MIE. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted. Results: Of the 251 patients included in this analysis, 200 patients underwent Ivor-Lewis MIE and 51 patients underwent McKeown MIE. The incidence of anastomotic leak, anastomotic stenosis and recurrent laryngeal nerve injury was significantly higher in the McKeown MIE group than that in the Ivor Lewis MIE group. The 30-day postoperative mortality rate was 1.2% (n ¼ 1) in the McKeown MIE group. Lymph nodes harvested were significantly more in the MIE-McKeown group than in Ivor Lewis MIE group (P < 0.05). The median follow-up period was 15 months (1e25 months) and the overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage 1), 83.8% (stage II), 73.4% (stage III). Conclusions: MIE for esophageal cancer according to the location and clinical stage of the tumor will decrease all postoperative complications and may yield the greatest benefit from surgery. © 2017 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Esophageal cancer Esophagectomy laparoscopy Thoracoscopy
1. Introduction Cancers arising from the esophagus are relatively common in
* Corresponding author. ** Corresponding author. E-mail addresses: [email protected] (D. Gao), [email protected] (L. Gao). 1 Drs. Chen and Liu contributed equally to this work.
China. Surgery is the primary therapy for esophageal cancer. However, traditional open esophagectomy carries significantly high risks of operative morbidity and mortality. Advances in surgical treatment have made minimally invasive esophagectomy (MIE) more popular and widely acceptable since the 1990s [1,2]. Currently, MIE can be performed through the laparoscopic transhiatal, the laparoscopicthoracoscopic Ivor Lewis, or the laparoscopic-thoracoscopic McKeown approach [3]. The prognosis for esophageal cancer is very poor with the
http://dx.doi.org/10.1016/j.amsu.2017.03.038 2049-0801/© 2017 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
median survival time ranging from 1 to 2 years [4]. Traditional open surgical transthoracic and transhiatal esophagectomies are associated with a relatively high morbidity and mortality rate which can impair quality of life [5,6]. In an effort to improve the outcomes associated with esophagectomy, minimally invasive approach to esophageal resection has been adopted [7e11]. The use of MIE approaches was associated with a shorter hospital stay, decreased morbidity and improved outcomes compared with open esophagectomy [12e18]. However, the rapid worldwide use of MIE approaches has not been followed by a rigorous scientific analysis of results. Large scale multicenter surgical clinical trials are difficult to conduct, and few studies have had sufficient follow-up to judge the long-term oncologic results. The numerous technical variables (including the patient's position - prone vs supine or the transoral anvil introduction vs the transthoracic route during an Ivor-Lewis esophagectomy) have jeopardized the results [19]. The ideal approach of MIE is not yet standardized. The potential benefits of McKeown MIE are a more proximal resection margin and improved lymph node dissection. However, these procedures are associated with a high complication rate and mortality, which is partly due to subtotal resection of esophagus, severe trauma, RLN injury and anastomotic leak, and stricture. And one recent study found that McKeown esophagectomy was an independent predictor of increased perioperative morbidity or mortality, independent of tumor histology. There are some advantages for MIE Ivor-Lewis approach such as the avoidance of subtotal resection of esophagus, the lower anastomotic leakage and stenosis, the better vascular supply of gastric conduit, and preliminarily good clinical outcomes. With the development of operative technic, the MIE Ivor-Lewis has become increasingly prevalent and is safe and feasible for patients with mid and lower esophageal cancer. In the present era of minimally invasive surgery, the choice among these approaches is mainly dominated by institutional preferences and clinical opinions. Until recently, the ideal approach of MIE is not yet standardized. The optimal approach should be tailored for each patient according to the location and clinical stage of the tumor [20]. The purpose of this study was to evaluate the effects of MIE approach according to the location of the tumor and to compare differences in perioperative and long term clinical outcomes between patients with cancer arising in the upper third of the esophagus and those with tumors involving the middle and lower third of the esophagus. 2. Patients and methods 2.1. Study design This was a prospective observation trial to evaluate the feasibility and outcomes of tailored therapy for each patient according to the location and the clinical stage of the tumor in an institution that had experience in minimally invasive surgical techniques. Feasibility was defined as the ability to carry out therapy without significant perioperative mortality. Patients included were those scheduled for MIE surgery at the Department of thoracic surgery Chinese PLA General Hospital. from January 2014 onwards. The medical charts were reviewed to obtain clinical data by using a standardized data collection sheet. Variables recorded included sex, age at the time of surgery, comorbid conditions, preoperative symptoms, operative details, and tumor-specific variables. All patients underwent esophagus-gastro-duodenoscopy, a thoracoabdominal CT scan and selective endoscopic ultrasound evaluation every 6 months. All the data was stored in a database that was analyzed for perioperative complications and long term outcomes in patients. The study was approved by the Ethics Committee of Chinese PLA General Hospital, Beijing, China.
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2.2. Pretreatment staging All patients underwent pretreatment staging according to the American Joint Committee on Cancer seventh edition criteria. Diagnostic investigations routinely included a history taking, physical examination, routine laboratory tests, a barium study and an oesophago-gastro-duodenoscopy with biopsies, a neck and thoracoabdominal CT scan, selective endoscopic ultrasound evaluation, and external ultrasonography of the neck, with fine-needle aspiration of lymph nodes when cancer was suspected. 2.3. Eligibility criteria Patients who were histologically proved suffering from esophageal carcinoma by taking biopsy specimens from the tumor during an endoscopy and the stomach was required to be available for use as a conduit were eligible for inclusion in the study. Patients with tumors of no clinical evidence of metastatic spread (M0) were enrolled. A complete evaluation of cardiac and respiratory functions was made, and all patients were found fit for operation and anesthesia. Informed consent was obtained from all patients. Exclusion criteria included patients with a prior antireflux or gastric operation. Patients who had a prior right thoracotomy or a prior major neck operation were excluded. Patients who were converted to an open procedure were also excluded. 2.4. Operative approach For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted (Group A). For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed (Group B). The distance between the incisal edge and the upper edge of the tumor is 5e7 cm. The operative technique has previously been described in detail elsewhere [21e24]. Two main operative techniques are adopted at our institution, namely a three-incision MIE with cervical anastomosis (MIE McKeown approach) and a two-incision MIE with intrathoracic anastomosis (MIE Ivor Lewis approach). After general anesthesia and endotracheal intubation, the patient was placed in the left lateral decubitus position. The surgeon stands on the right and the assistant on the left. Three ports were placed in the 7th intercostal space at mid-axillary line, the 5th intercostal space at the anterior axillary line and in scapular line at the 8th intercostal space respectively. In short, MIE McKeown approach consists of mobilizing the thoracic esophagus from the hiatus to the thoracic inlet, intrathoracic lymphadenectomy and cervical anastomosis. A staging laparoscopy was performed in the same setting or as a separate procedure to ensure resectability in most patients. Neck wound is closed in layers after placing a corrugated drain. Laparoscopic and thoracoscopic dissection is also performed and followed by a side-to-side stapled thoracic anastomosis for the MIE Ivor Lewis approach [12]. Lymph nodes along left gastric artery and the lesser curvature of the stomach, mediastinal lymph nodes, abdominal lymph nodes that included paracardial lymph nodes, with bilateral recurrent nerve lymph nodes were routinely dissected. If the primary tumor was located between the upper and mid-thoracic esophagus, supraclavicular lymph nodes were dissected simultaneously. A feeding jejunostomy tube is placed laparoscopically in most of the patients. One tube-drain is placed close to hiatus, trocars are removed, and ports are closed. Patients are extubated in the operating room. The patients post-operation were given parenteral nutrition through the deep vein or through a nasogastric tube. Patients are discharged on tube feed support with a full liquid diet.
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For patients with positive lymph node metastasis in a resected specimen, adjuvant chemotherapy using 5-fluororouracil and cisplatin every 3 weeks for two cycles was administered.
Survival curves during follow-up were plotted by the Kaplane Meier method. Significance was considered to be present for values of p < 0.05. A commercial statistical software package (SPSS for Windows, version 17.0; SPSS, Chicago, IL) was used for data analysis.
2.6. Perioperative and postoperative outcomes
3. Results
All patients surviving operation were followed until death or time of database closure (January 2016). Perioperative and postoperative data were record, including duration of surgery, blood loss, and postoperative length of stay, surgical outcomes, postoperative complications, operative mortality, recurrence and hospital and late morbidity and mortality. The primary endpoint of this study was all cause mortality. Secondary endpoints were operative and postoperative major morbidity.
3.1. Participants
2.5. Adjuvant chemotherapy
2.7. Statistical analysis Data are reported as the mean ± SD for continuous variables and as frequencies for categorical variables. Continuous variables were compared by Student t-test for normally distributed values. Differences in percentages were evaluated using the Chi-square test.
The study was started in January 2014. We enrolled 258 patients. Two patients were converted to open surgery for bleeding. One patient withdrew consent after registration. Of the remaining 255 patients, two patients had a prior right thoracotomy, one patient had a prior gastric operation, and one patient did not undergo resection, leaving 251 patients eligible for the analysis (Fig. 1). Clinical characteristics of the patients with tumor arising in the middle and lower third of the esophagus (Group A) and the patients with esophageal cancer arising in the upper third of the esophagus (Group B) are listed in Table 1. The total number of included cases was 251, and the male/female ratio was approximately 4:1. At presentation, 47 patients had comorbid conditions in the form of diabetes and 49 patients suffered from coronary artery disease. Of
Fig. 1. Consort diagram.
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
57
Table 1 Characteristics of patients who underwent esophagectomy: Comparing MIE-McKeown and MIE-Ivor Lewis. Preoperative characteristics
Group A (n ¼ 200)
Group B (n ¼ 51)
Total, n ¼ 251
P
Age (years) Sex (Male) BMI, kg/m2, median (IQR) Pretreatment weight loss, n (%) Comorbid conditions History of gastroesophageal reflux disease Diabetes mellitus, n (%) Coronary artery disease, n (%) COPD/emphysema, n (%) Chronic renal insufficiency, baseline Cr > 2 mg/dL or HD, n (%) Smoking history Current Former Never
59.9 ± 8.4 169 (84.5%) 23.5 (20.1e26.8) 81 (40.5)
61.4 ± 9.1 38 (74.7%) 22.9 (20.8e25.4) 20 (38.6)
60.4 ± 8.7 207 (82.5%) 23.1 (21.0e26.8) 101 (40.2)
0.192 0.102 0.134 1.000
152 (76.0) 37 (18.5) 40 (20.0) 44 (22.0) 4 (2.0)
40 (78.4) 10 (19.6) 9 (17.6) 12 (23.5) 1 (2.0)
192 (76.9) 47 (18.7) 49 (19.5) 56 (22.3) 5 (2.0)
0.854 0.842 0.844 0.851 1.000
28 (14) 118 (59.0) 54 (27.0)
6 (11.7) 24 (47.1) 21 (41.2)
34 (13.6) 142 (56.6) 75 (29.8)
0.820 0.202 0.059
BMI indicates body mass index; HD, hemodialysis.
the 251 patients with esophageal cancer, 155 (61.7%) patients had dysphagia. All patients were histologically proved suffering from esophageal carcinoma and had clear indications and clinical purpose for MIE. Preoperative nutrition of these patients was maintained by high protein calorie liquid or soft diet. The demographic characteristics were similar between two groups.
chylothorax, cardiac arrhythmia, ICU length of stay and hospital length of stay between two groups. There were no intraoperative mortalities. The 30-day postoperative mortality rate was 1.2% (n ¼ 1) in the McKeown MIE group. This patient died of multiple organ dysfunction syndromes resulting from anastomotic leakage which was confirmed by gastrograf in swallow.
3.2. Operative and postoperative details 3.3. Pathologic findings For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed. For tumors involving the middle and lower third of the esophagus, MIE Ivor Lewis approach was adopted. Intraoperative and postoperative data of patients are presented in Table 2. Anastomotic leak was detected in eight patients. The leak was minor and managed conservatively. Three patients experienced hoarseness of voice reflecting recurrent laryngeal injury (paresis), which resolved within 5 weeks. Three patients (1.2%) required conversion to open thoracotomy due to adhesions or emergency thoracotomy for bleeding. One patient died of anastomotic leakage postoperatively. Twelve patients experienced long-term complications in the form of stenosis, with dysphagia that required serial dilations. The mean operative time of McKeown MIE group is significant shorter than the Ivor Lewis MIE group (296.1 ± 35.9s vs. 322.8 ± 50.5s, p ¼ 0.013, respectively). However, the occurrence of anastomotic leak, anastomotic stenosis and RLN injury in the McKeown MIE group was significant higher than those in the Ivor Lewis MIE group. There was no statistical significance with the blood loss, adequacy of cancer resection, reoperations, disparity of
Table 2 Technical and perioperative aspects of patients: Comparing MIE-Ivor Lewis and MIEMcKeown.
Duration of surgery (min) Blood loss (ml) Conversion to open, n (%) Reoperations, n (%) Anastomotic leakage, n (%) Anastomotic stenosis, n (%) RLN injury, n (%) Pulmonary complications Chylothorax, n (%) Cardiac arrhythmia, n (%) ICU stay, n (%) Hospital length of stay (d) Mortality at 30 days, n (%) RLN, recurrent laryngeal nerve.
Group A (n ¼ 200)
Group B (n ¼ 51)
P
322.8 ± 50.5 181.5 ± 80.0 2 (1.0) 2 (1.0) 1 (0.5) 2 (1.0) 0 (0) 10 (5.0) 0 (0) 6 (3.0) 3 (1.5) 16.7 ± 5.5 0 (0)
296.1 ± 35.9 172.6 ± 90.1 1 (2.0) 2 (3.9) 4 (7.8) 6 (11.8) 3 (5.9) 8 (15.7) 1 (1.9) 2 (3.9) 2 (3.9) 18.6 ± 6.5 1 (2.0)
0.013 0.594 0.496 0.184 0.007 0.001 0.008 0.103 0.203 0.666 0.268 0.621 0.203
For 215 patients (85.7%), the malignancy was squamous cell cancer. Twenty-eight patients (11.2%) had adenocarcinoma. Six patients had neuroendocrine carcinoma. The remaining 2 patients had Melanoma (Table 3). Lymph nodes harvested were significantly more in the MIE-McKeown group than that of in Ivor Lewis MIE group (P < 0.05). There was no significant difference in the R0 resection rate between groups A and B (95.0%vs. 96.1%). As shown in Table 3, 129 patients were pathologically positive for LN metastasis, which was evaluated as an indication for adjuvant chemotherapy. Of these 129 patients, 98 (76%) received adjuvant chemotherapy. The remaining 31 (24%) patients did not receive chemotherapy because of age (n ¼ 12, 9.3%), other cancer diagnosis (n ¼ 8, 6.2%), postoperative complications (n ¼ 6, 4.7%), and patient's instances (n ¼ 5, 3.9%). 3.4. Clinical outcomes Follow-up was 100% complete in 251 patients. No patient was lost to follow-up. The median follow-up period was 15 months (range, 1e25 months). The overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage I), 83.8% (stage II), 73.4% (stage III). Survival by pathological stage is demonstrated in Fig. 2. Survival by pathological stage and operation procedures are demonstrated in Figs. 3 and 4. Recurrence was mainly systemic in the form of liver and lung metastasis. At this writing, no patient has had any intrathoracic recurrence. 4. Discussion This experience has demonstrated that MIE can be performed safely without intraoperative mortality, with ICU stay rate of 2.0% (n ¼ 5) and a median hospital stay of 17 days. MIE procedure was better than most published series of open esophagectomy [5]. In our comparison of short-term and long-term outcomes between the MIE-chest and MIE-neck groups, the mean operative time of McKeown MIE group is significant shorter than the Ivor Lewis MIE group (p ¼ 0.013). However, the occurrence of anastomotic leak,
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L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60 Table 3 Pathologic findings after operation: Comparing MIE-Ivor Lewis and MIE-McKeown. Tumor specific variables AJCC stage, n (%) I IIa IIb III Squamous tumor type, n (%) Adenocarcinoma tumor type, n (%) Neuroendocrine carcinoma, n (%) Melanoma, n (%) Adequacy of cancer resection Negative margins, n (%) Lymph nodes harvested(n) Lymph nodes metastasis rate, n (%) Adjuvant chemotherapy n (%)
Group A (n ¼ 200)
Group B (n ¼ 51)
P
20 (10.0) 53 (26.5) 48 (24.0) 99 (49.5) 170 (85.0) 24 (12.0) 4 (2.0) 2 (1.0)
7 (13.7) 11 (21.6) 11 (21.6) 22 (43.1) 45 (88.2) 4 (7.9) 2 (3.9) 0 (0)
0.451 0.590 0.854 0.437 0.659 0.618 0.605 1.000
190 (95.0) 19.5 ± 9.6 105 (52.5) 80 (40.0)
49 (96.1) 27.5 ± 10.1 24 (47.1) 18 (35.3)
0.496 0.031 0.532 0.562
AJCC, American Joint Committee on Cancer.
Fig. 2. KaplaneMeier plot of the estimated overall survival of patients stratified by stage.
anastomotic stenosis and RLN injury in the McKeown MIE group was significant higher than those in the Ivor Lewis MIE group. These findings are consistent with the first prospective multicenter study of MIE [7]. In the present study, we choose the approach of MIE according to the location of the tumor. Ivor-Lewis MIE approach is used for the treatment of mid and lower esophageal cancers, and with fewer complications such as RLN injury, anastomosis leak and anastomosis stenosis. These findings are consistent with other reported studies [12,24e28]. The lower rate of anastomosis leak in the MIE Ivor-Lewis group mainly due to the reduced tension at the anastomosis and the ability to remove the potentially ischemic gastric tip. However, Ivor-Lewis MIE is technically demanding and requires extensive experience. For cancer arising in the upper third of the esophagus, MIE McKeown approach was performed in our study. The main cause is the intrathoracic anastomosis and the embedding of the staple line in the MIE Ivor-Lewis group are more complex and waste more time. Significantly, more lymph nodes were resected in patients who underwent McKeown MIE in the present study (P < 0.05). The extent of lymph node dissection required for patients with esophageal cancer also remains controversial [29,30]. However,
Fig. 3. KaplaneMeier plot of the estimated overall survival of patients who accepted MIE-Ivor Lewis operation, stratified by stage.
Fig. 4. KaplaneMeier plot of the estimated overall survival of patients who accepted MIE-McKeown operation, stratified by stage.
L. Chen et al. / Annals of Medicine and Surgery 17 (2017) 54e60
adequate lymph node sampling is required for accurate staging [30]. One of the potential advantages of the McKeown MIE approach is better exposure and improved cervical lymphadenectomy. Esophagectomy is a complex and technically challenging operation. Specialty training of the surgeon and surgeon volume has an impact on clinical outcomes. In the current study, the operative time was significantly different between two groups (322.8 ± 50.5vs. 296.1 ± 35.9) because the intrathoracic anastomosis and the embedding of the staple line in the MIE Ivor-Lewis group were more complex and wasted more time. Intrathoracic anastomosis is technically demanding and learning curve is relatively long. McKeown approach avoids the most difficult problem of intrathoracic anastomosis. Cervical anastomosis is relatively simple and easy to operate. Thus, the MIE McKeown approach is more convenient and easier to grasp for the beginners. In the reports of experienced centers, open esophagectomy approaches are frequently associated with significant morbidity and a mortality rate in the range of 6e23% [31,32]. In one study of 1777 patients undergoing open esophagectomy, the most frequent reported complications were pneumonia (21%), respiratory failure (16%) and prolonged ventilator support (22%) [33]. Given concerns over this high morbidity and mortality, minimally invasive esophagectomy has been performed with increasing frequency. Our mortality of 0.4% and the low incidence of pneumonia (7.17%) and RLN injury (1.2%) suggest an advantage for the MIE. At a median follow-up of 15 months, no significant difference in survival was noted between the two groups of patients. The overall survival rate at 1 year stratified by pathologic stage at esophagectomy was 95.9% (stage I), 83.8% (stage II), 73.4% (stage III). Furthermore, the oncological outcomes in the current study were good with an estimated 1-year overall survival of 81.7%. The estimated overall survival is acceptable when compared with published series of open esophagectomy. These results suggest that MIE can provide equivalent oncological outcomes as compared with open transthoracic esophagectomy.
4.1. Strength and limitations The study is prospective trial designed to investigate the effects of MIE approach according to the location of tumor and compare the clinical outcomes between the Ivor Lewis and McKeown MIE procedures. However, there are several limitations in this study. Firstly, the main problem is the relative low proportion of upper third of the esophagus, thus may limited the statistical power. Secondly, the optimal approach to esophagectomy is controversial. The selection of MIE approach is lack of standard and is mainly based on the location of the tumor. Thirdly, the median follow-up period was short and lack of exploration of the long-term effects, especially on quality of life. Longer follow-up period is required to fully evaluate the oncologic results of MIE. it is a single-institution study. Largescale, prospective multicenter trials are required to fully judge the long-term results of MIE.
Ethical approval The study was approved by the Ethics Committee of Chinese PLA General Hospital, Beijing, China.
Sources of funding This work was supported by a general financial grant from the China Postdoctoral Science Foundation (2012T50865, to L. Gao.).
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Author contribution Chen L, Gao LG, Wang R, Liu X and Gao DW contributed to the study design, data collections. Chen L, Zhang T, Liu X contributed to the data analysis, writing. Conflicts of interest The authors declare no conflict of interest. Guarantor Gao DW. Research registration unique identifying number (UIN) Researchregistry1949. Acknowledgment This work was supported by a general financial grant from the China Postdoctoral Science Foundation (2012T50865, to L. Gao.). References [1] O.J. McAnena, J. Rogers, N.S. Williams, Right thoracoscopically assisted oesophagectomy for cancer, Br. J. Surg. 81 (1994) 236e238. [2] S. Law, M. Fok, K.M. Chu, J. Wong, Thoracoscopic esophagectomy for esophageal cancer, Surgery 122 (1997) 8e14. [3] B.A. Yerokun, Z. Sun, C.F. Jeffrey Yang, B.C. Gulack, P.J. Speicher, M.A. Adam, et al., Minimally invasive versus open esophagectomy for esophageal cancer: a population-based analysis, Ann. Thorac. Surg. 102 (2016) 416e423. [4] A. Ayiomamitis, Epidemiology of cancer of the esophagus in Canada: 19311984, Gastroenterology 94 (1988) 374e380. [5] S.H. Bailey, D.A. Bull, D.H. Harpole, J.J. Rentz, L.A. Neumayer, T.N. Pappas, et al., Outcomes after esophagectomy: a ten-year prospective cohort, Ann. Thorac. Surg. 75 (2003) 217e222 discussion 22. [6] J.D. Birkmeyer, A.E. Siewers, E.V. Finlayson, T.A. Stukel, F.L. Lucas, I. Batista, et al., Hospital volume and surgical mortality in the United States, N. Engl. J. Med. 346 (2002) 1128e1137. [7] J.D. Luketich, A. Pennathur, Y. Franchetti, P.J. Catalano, S. Swanson, D.J. Sugarbaker, et al., Minimally invasive esophagectomy: results of a prospective phase II multicenter trial-the eastern cooperative oncology group (E2202) study, Ann. Surg. 261 (2015) 702e707. [8] J.D. Luketich, M. Alvelo-Rivera, P.O. Buenaventura, N.A. Christie, J.S. McCaughan, V.R. Litle, et al., Minimally invasive esophagectomy: outcomes in 222 patients, Ann. Surg. 238 (2003) 486e494 discussion 94e95. [9] T. Irino, J.A. Tsai, J. Ericson, M. Nilsson, L. Lundell, I. Rouvelas, Thoracoscopic side-to-side esophagogastrostomy by use of linear stapler-a simplified technique facilitating a minimally invasive Ivor-Lewis operation, Langenbecks Arch. Surg. 401 (2016) 315e322. [10] S. Sihag, A.S. Kosinski, H.A. Gaissert, C.D. Wright, P.H. Schipper, Minimally invasive versus open esophagectomy for esophageal cancer: a comparison of early surgical outcomes from the society of thoracic surgeons national database, Ann. Thorac. Surg. 101 (2016) 1281e1289. [11] P. Xiao, X. Zhuang, Y. Shen, Q. Li, W. Dai, X.J. Yang, et al., Reverse-puncture anastomotic technique for minimally invasive Ivor-Lewis esophagectomy, Ann. Thorac. Surg. 100 (2015) 2372e2375. [12] J.D. Luketich, A. Pennathur, O. Awais, R.M. Levy, S. Keeley, M. Shende, et al., Outcomes after minimally invasive esophagectomy: review of over 1000 patients, Ann. Surg. 256 (2012) 95e103. [13] M.R. Xie, C.Q. Liu, M.F. Guo, X.Y. Mei, X.H. Sun, M.Q. Xu, Short-term outcomes of minimally invasive Ivor-Lewis esophagectomy for esophageal cancer, Ann. Thorac. Surg. 97 (2014) 1721e1727. [14] K. Kim, J.S. Park, H. Seo, Early outcomes of video-assisted thoracic surgery (VATS) Ivor Lewis operation for esophageal squamous cell carcinoma: the extracorporeal anastomosis technique, Surg. Laparosc. Endosc. Percutan Tech. 23 (2013) 303e308. [15] J. Mu, Z. Yuan, B. Zhang, N. Li, F. Lyu, Y. Mao, et al., Comparative study of minimally invasive versus open esophagectomy for esophageal cancer in a single cancer center, Chin. Med. J. Engl. 127 (2014) 747e752. [16] C. Palanivelu, A. Prakash, R. Senthilkumar, P. Senthilnathan, R. Parthasarathi, P.S. Rajan, et al., Minimally invasive esophagectomy: thoracoscopic mobilization of the esophagus and mediastinal lymphadenectomy in prone positioneexperience of 130 patients, J. Am. Coll. Surg. 203 (2006) 7e16. [17] A.I. Lazzarino, K. Nagpal, A. Bottle, O. Faiz, K. Moorthy, P. Aylin, Open versus minimally invasive esophagectomy: trends of utilization and associated
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